Variant #0000865904 (NC_000019.9:g.1397362C>G, NM_000156.5:c.707G>C (GAMT))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1397362C>G
DNA change (hg38) -
Published as GAMT(NM_000156.5):c.707G>C (p.G236A)
ISCN -
DB-ID NDUFS7_000031
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAMT NM_000156.5 -?/. - c.707G>C r.(?) p.(Gly236Ala)
NDUFS7 NM_024407.4 -?/. - c.*1875C>G r.(=) p.(=)


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